Back to EveryPatent.com
| United States Patent |
5,789,639
|
|
Itoh
|
August 4, 1998
|
Process for manufacturing alkenyl compounds
Abstract
A process for manufacturing an alkenyl compound which comprises reacting an
alkylbenzene and 1,3-butadiene in the presence of metallic sodium or a
combination of metallic sodium and an oxide, a hydroxide, or a salt of
potassium, rubidium or an alkaline earth metal, or a mixture of these
under a pressure of 1 kPa (gauge) to 30 MPa (gauge). The process can
produce alkenyl compound which is an industrially valuable compound as a
raw material for the manufacture of naphthalenedicarboxylic acid, a highly
useful raw material of polymers, at a high yield using a small amount of
metallic sodium.
| Inventors:
|
Itoh; Takashi (Satte, JP)
|
| Assignee:
|
Cosmo Oil Co., Ltd. (Tokyo, JP);
Petroleum Energy Center (Tokyo, JP)
|
| Appl. No.:
|
502648 |
| Filed:
|
July 14, 1995 |
Foreign Application Priority Data
| Jul 20, 1994[JP] | 6-190080 |
| Dec 22, 1994[JP] | 6-336045 |
| Current U.S. Class: |
585/452; 585/435; 585/438; 585/446; 585/467; 585/802 |
| Intern'l Class: |
C07C 002/64; C07C 005/09; C07C 015/46; C07C 007/00 |
| Field of Search: |
585/435,446,452,467,438,802
|
References Cited
U.S. Patent Documents
| 3953535 | Apr., 1976 | Shima et al. | 585/452.
|
| 3954895 | May., 1976 | Shima et al. | 585/452.
|
| 3954896 | May., 1976 | Shima et al. | 585/438.
|
| 4018840 | Apr., 1977 | Iwata et al. | 585/432.
|
| 5329058 | Jul., 1994 | Shimada et al. | 585/438.
|
| 5523504 | Jun., 1996 | Itoh | 585/438.
|
| 5527977 | Jun., 1996 | Takagawa et al. | 585/802.
|
Primary Examiner: Caldarola; Glenn
Assistant Examiner: Hailey; Patricia L.
Attorney, Agent or Firm: Oblon, Spivak, McClelland, Maier & Neustadt, P.C.
Claims
I claim:
1. A process for manufacturing an alkenyl compound which comprises reacting
an alkylbenzene and 1,3-butadiene in the presence of metallic sodium as
sole catalyst under a pressure of 10 kPa (gauge) to 1 MPa (gauge).
2. The process according to claim 1, wherein the amount of metallic sodium
used for the reaction is 0.001-2% by weight of the total amount of
alkylbenzene and 1,3-butadiene.
3. The process according to claim 1, wherein the alkylbenzene is toluene,
ethylbenzene, o-xylene, m-xylene, p-xylene, trimethylbenzene,
tetramethylbenzene, or pentamethylbenzene.
4. The process according to claim 1, wherein the ratio of
alkylbenzene:1,3-butadiene is 1:0.001 to 1:0.5.
5. The process according to claim 1, wherein the reaction is carried out
substantially in the absence of water and oxygen.
6. The process according to claim 1, wherein the metallic sodium is molded
together with a porous material.
7. The process according to claim 6, wherein the porous material is
selected from the group consisting of alumina, silica, silica alumina,
X-zeolite, Y-zeolite, mordenite, pentasyl zeolite, L-zeolite,
ion-exchanged resin, montmollilonite, and sepiolite.
Description
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a process for manufacturing an alkenyl
compound which is an industrially valuable compound as a raw material for
the manufacture of naphthalenedicarboxylic acid, a highly useful raw
material of polymers such as polyethylene naphthalate (PEN).
2. Description of the Background Art
In the process for manufacturing alkenyl compounds, an alkylbenzene and
1,3-butadiene are reacted in the presence of an alkali metal as a
catalyst. Conventionally known catalysts used in this reaction are
metallic potassium (Japanese Patent Publication (kokoku) No. 17973/1975)
and a combination of metallic potassium and metallic sodium (Japanese
Patent Publication (kokoku) Nos. 34570/1981, 26489/1982, and 17973/1975).
Conventional methods using these catalysts, however, have the following
drawbacks.
(1) High production cost due to the use of expensive metallic potassium.
(2) Risks associated with the use of metallic potassium. Metallic potassium
is highly reactive with water, moist air, and the like, and is thus
ignited by merely bringing it to come into contact with them. Thus, it may
ignite combustible materials, such as raw materials and reaction products.
These methods are therefore very dangerous because of the use of metallic
potassium which has these characteristics.
In an effort of avoiding the use of metallic potassium, a method of using
metallic sodium and an inorganic salt of potassium has been proposed
(Japanese Patent Laid-open (kokai) Nos. 31935/1972, 226927/1992, and WO
91-16284).
This method does not necessarily provide industrial advantage because of
(3) the requirement for special agitators, such as an emulsification
apparatus, and the requirement for the use of high purity inorganic salt
of potassium.
Japanese Patent Application Laid-open (kokai) No. 107569/1994 discloses a
method which does not require the use of the special agitators. This
patent application claims that even though the reaction is caused to
proceed very little when metallic sodium and an inorganic salt of
potassium are used as a catalyst while stirring the mixture using a
stirrer equipped with half-moon-shaped blades, the reaction yield is
greatly improved if glass balls or .alpha.-alumina balls which scrape away
the surface of powdery catalysts are used together.
This method, however, has a problem that (4) rotation of the stirring
blades is disturbed, causing the equipment to be unduly abraded, due to
the use of glass balls or .alpha.-alumina balls with a large average
diameter (about 2.0-3.0 mm).
In addition, a method of using only metallic sodium is known (Dimitrror Ch.
et al. Dokl. Bolg Akad. Nuak., 33, 353 (1980)).
This method (5) requires a large amount of metallic sodium, e.g. 7.9% by
weight of o-xylene, and yet gives only an extremely low yield, e.g. 31.6%.
An object of the present invention is therefore to provide a process for
manufacturing an alkenyl compound from an alkylbenzene and 1,3-butadiene,
which is free from all the problems (1)-(5) above.
As a result of extensive studies for achieving this object, the present
inventor has found that a reaction of alkylbenzene and 1,3-butadiene under
a certain prescribed pressure in the presence of a catalyst system
consisting of metallic sodium alone or a combination of metallic sodium
and an oxide, a hydroxide, or a salt of potassium, rubidium or an alkaline
earth metal, or a mixture of these, produced the alkenyl aromatic compound
at a high yield without using a large amount of metallic sodium.
SUMMARY OF THE INVENTION
Accordingly an object of the present invention is to provide a process for
manufacturing an alkenyl compound which comprises reacting an alkylbenzene
and 1,3-butadiene in the presence of metallic sodium under a pressure of 1
kPa (gauge) to 30 MPa (gauge).
Another object of the present invention is to provide a process for
manufacturing an alkenyl compound which comprises reacting an alkylbenzene
and 1,3-butadiene in the presence of metallic sodium and an oxide, a
hydroxide, or a salt of potassium, rubidium or an alkaline earth metal, or
a mixture of these, under a pressure of 1 kPa (gauge) to 30 MPa (gauge),
said reaction is carried out in the presence of, in addition to the
metallic sodium,
Other and further objects, features and advantages of the present invention
will appear more fully from the following description.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a drawing illustrating one embodiment of the device for carrying
out the process of the present invention.
DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS
The alkylbenzene in the present invention denotes a compound having 1-5
groups selected from alkyl groups such as methyl group and ethyl group on
benzene ring. Toluene, ethylbenzene, o-xylene, m-xylene, p-xylene,
trimethylbenzene, tetramethylbenzene, and pentamethylbenzene, are given as
specific examples.
It is desirable that one of these alkylbenzenes be used alone. If two or
more of them are used together, it is difficult to separate each target
compound at a high purity from alkenyl compounds produced by the reaction.
Further, it is desirable for the purpose of effective isolation of target
compound to use an alkylbenzene with a purity as high as possible. A
specific desirable purity is 95% or higher, and especially 98% or higher.
Notwithstanding this stringent purity requirement for alkylbenzene,
inclusion of a slight amount of hydrocarbons having no alkyl groups, such
as benzene and cyclohexane, is acceptable.
Alkylbenzene with a water content as low as possible is preferred, because
the water impairs the catalyst by reducing the activity of metallic
sodium. A preferred water content is below the detectable sensitivity by
Karl Fischer's method which is a common measuring method of a water
content, and specifically it is below several ppm.
The use of dehydrated alkylbenzene is therefore preferred.
The method for dehydrating alkylbenzenes which can be employed include a
method of absorbing and separating water using an appropriate drying
agent, such as activated alumina, silica gel, molecular sieve, or
activated carbon; a low temperature separation method; and a method of
contacting alkylbenzenes with metallic sodium or metallic potassium. Among
these, the last-mentioned method, i.e. the method of contacting
alkylbenzenes with metallic sodium or metallic potassium, is preferred.
There are no limitations as to the method for manufacturing 1,3-butadiene
to be reacted with alkylbenzene. There are also no need for the purity of
the 1,3-butadiene to be as high as the above-mentioned purity of
alkylbenzene. The reaction proceeds smoothly and there are no needs for
isolation of the target compound irrespective of the purity of
1,3-butadiene. Crude butadiene obtained, for example, by the
dehydrogenation of butane or butene can be used as is, or 1,3-butadiene
obtained by purification of this crude butadiene by extraction or the like
can be also used.
Nevertheless, a lower water content of 1,3-butadiene is more desirable from
the same reasons as mentioned above in connection with alkylbenzenes.
Specifically, a preferred water content of 1,3-butadiene is several ppm.
Thus, the use of dehydrated 1,3-butadiene is preferred.
The method for dehydrating 1,3-butadiene which can be employed include a
method of absorbing and separating water using an appropriate drying
agent, such as activated alumina, silica gel, molecular sieve, or
activated carbon; and a low temperature separation method.
It is desirable that metallic sodium which is the catalyst for the reaction
of alkylbenzene and 1,3-butadiene has a high purity, although it may
contain a slight amount of calcium, magnesium, and potassium. The purity
of 90% or higher, especially 99.0% or higher, is preferred.
The amount of metallic sodium used for the reaction is 0.001-2% by weight,
preferably 0.005-1% by weight, and more preferably 0.05-1% by weight, of
the total amount of the alkylbenzene and 1,3-butadiene to be reacted. If
the amount of metallic sodium is less than 0.001% by weight, the catalytic
activity is insufficient, while the amount greater than 2% by weight does
not bring about any effects proportional to the excess amount.
In another embodiment of the present invention, a catalyst system
comprising, in addition to the metallic sodium, an oxide, a hydroxide, or
a salt of potassium, rubidium or an alkaline earth metal, or a mixture of
these (hereinafter collectively referred to as "specific catalyst
component") can be used for carrying out the above reaction. In this
instance, the metallic sodium is preferably dispersed in the specific
catalyst component.
Given as examples of the specific catalyst component are potassium oxide,
potassium hydroxide, potassium carbonate, potassium sulfate, potassium
chloride, potassium aluminate, rubidium oxide, rubidium hydroxide,
rubidium carbonate, rubidium sulfate, calcium oxide, calcium hydroxide,
calcium carbonate, calcium sulfate, calcium chloride, magnesium oxide,
magnesium hydroxide, magnesium carbonate, magnesium sulfate, magnesium
chloride, and the like. These specific catalyst components may be used
either alone or in combination of two or more. Among these, preferred
specific catalyst components are potassium hydroxide, potassium carbonate,
potassium chloride, rubidium hydroxide, rubidium carbonate, calcium
hydroxide, and calcium carbonate.
These specific catalyst components may contain sodium salts, such as sodium
carbonate and sodium chloride, at a weight ratio of the specific catalyst
components: sodium salts of about 10:1 to 1:10, preferably about 10:1 to
1:1. Inclusion of sodium salts in the specific catalyst component may
occasionally promote the function of the catalyst used in the process of
the present invention.
These specific catalyst components (hereinafter the "specific catalyst
component" denotes those which may contain sodium salts) should be
sufficiently dry. In particular, it is preferable that these specific
catalyst components be sufficiently calcined at a high temperature of
200.degree. C. to 600.degree. C. in order to adequately promote their
activity. Further, the specific catalyst components are preferably
particles with a mean diameter of 100 .mu.m or smaller, particularly 10 to
50 .mu.m. Adjustment of the particle size can be carried out by sieve or
the like.
Although there are no specific limitations to the ratio of metallic sodium
and the specific catalyst component, the amount of metallic sodium is
adjusted to have its final content in the catalyst of 0.1 to 30% by
weight, preferably 0.5 to 20% by weight, and particularly preferably 1 to
10% by weight. If the amount of metallic sodium is smaller than 0.1 by
weight, the action of the catalyst in the present invention is
insufficient. The amount of metallic sodium greater than 30% by weight
brings about no catalytic effects proportionate to the added amount, and
only makes the process uneconomical.
A typical method of dispersing metallic sodium and the specific catalyst
component comprises dispersing fine particles of metallic sodium and the
specific catalyst component together. The dispersion-supporting is
preferably carried out in an inert solvent. The master batch method or the
method of preparing suspensions, each containing the metallic sodium or
the specific catalyst component, and mixing the two suspensions are
employed for homogeneously dispersing 0.1-30% by weight of metallic sodium
and the specific catalyst component by dispersion-supporting in an inert
solvent.
For example, in the case where 3% by weight of metallic sodium is dispersed
in the specific catalyst component, 3 parts by weight of metallic sodium
and 97 parts by weight of the specific catalyst component are together put
into 1333 parts by weight of a solvent (alkylbenzene) and the mixture is
stirred at a high speed at 110.degree.-130.degree. C. Alternatively, a
suspension containing metallic sodium and the specific catalyst component
at a suitable ratio is prepared in advance, and this suspension is further
dispersed by the remaining specific catalyst component in the solvent
(alkylbenzene).
Another method for the dispersion-supporting is mixing a suspension of 3
parts by weight of metallic sodium in 333 parts by weight of alkylbenzene
and a suspension of 97 parts by weight of the specific catalyst component
in 1000 parts by weight of alkylbenzene.
Still another method is preparing a suspension of 3 parts by weight of
metallic sodium and 47 parts by weight of the specific catalyst component
in 500 parts by weight of alkylbenzene and another suspension of 50 parts
by weight of the specific catalyst component in 833 parts by weight of
alkylbenzene, and then mixing the two suspensions.
In the industrial application of the inert solvent dispersion-supporting
method, the same alkylbenzene as the raw material is preferably used as
the solvent.
When the metallic sodium or a mixture of metallic sodium and the specific
catalyst component is desired to be held fixed, such as the case where the
reaction-distillation as hereinafter described is carried out, a molded
catalyst made from a porous material with the metallic sodium or the
mixture of metallic sodium and the specific catalyst component supported
thereon can be used.
Besides the compounds mentioned above, faujasite X-zeolite and Y-zeolite,
ion-exchanged mordenite, L-zeolite, potassium ion-exchanged resin, and the
like can be used as the specific catalyst component. Because these are
porous materials themselves, there are no need to use a separate porous
material for supporting the catalytic component.
Given as examples of porous materials for holding the catalyst, are
alumina, silica, silica alumina, X- and Y-zeolite, mordenite, pentasyl
zeolite such as ZSM-5, L-zeolite, ion-exchanged resin, and naturally
occurring clay minerals such as montmollilonite and sepiolite.
The following methods can be employed for supporting the metallic sodium or
the mixture of metallic sodium and the specific catalyst component on a
porous material.
One of the methods comprises molding the specific catalyst component,
calcined in advance to a degree where there is no substantial amount of
water contained therein, alone when the specific catalyst component is a
porous material, or together with the porous material when the specific
catalyst component is not a porous material, to produce molded particles
with a particle size of 1.6 mm (1/8") or larger, followed by calcining the
molded particles at 200.degree.-500.degree. C. In this instance, when
molded particles in the shape of a ring, a saddle, or the like are
desired, a molding binder, such as silica sol or alumina sol, can be used.
As the molding method, tablet method, casting method, extrusion, or the
like can be used with no specific limitations.
The particle size is not necessarily limited to 1.6 mm or larger. It is
possible to use smaller size particles, e.g. as small as about 0.1 mm, by
the same method of preparation mentioned above. However, in the case where
the particle size is small, e.g. 0.1-1.6 mm, these particles are desirably
filled in mesh containers, such as containers made from cloth, metallic
wires, glasses fibers, polymer fibers, or the like, in order to avoid
decrease in the fractionation distillation efficiency due to pressure loss
caused by the small size particles. These types of containers are
disclosed in U.S. Pat. No. 4,232,530, U.S. Pat. No. 4,242,530, U.S. Pat.
No. 4,250,052, U.S. Pat. No. 4,302,356, and U.S. Pat. No. 4,307,251.
The following methods can be employed for carrying metallic sodium on the
calcined dry material. One is a dry method which comprises saturating
metallic sodium, melted at 65.degree. to 700.degree. C., preferably at
100.degree. to 600.degree. C., and more preferably at 200.degree. to
500.degree. C., in a dehydrated carrier gas inert to the metallic sodium,
such as nitrogen, helium, or argon, and causing the melted metallic sodium
to come into contact with the calcined dry material. The other is a wet
method causing the melted metallic sodium as is or dispersed in an inert
solvent to come into contact with the calcined dry material. Normal
paraffins having 8-16 carbon atoms, alkylbenzenes, alkylnaphthalenes, or
the like can be used as the solvent in the wet method. Of these,
alkylbenzene, which is the raw material, is preferably used. The contact
temperature in the wet method is preferably above the melting point of
metallic sodium (97.8.degree. C.) and below the boiling point of the
solvent.
The catalyst with voids of 20 to 65 vol %, particularly 30 to 60 vol %, is
preferably used in the process of the present invention.
The reaction of process of the present invention using the catalyst
consisting of metallic sodium alone or a combination of the metallic
sodium and the specific catalyst component is carried out under the
pressure is 1 kPa (gauge) to 30 MPa (gauge), preferably 1 kPa (gauge) to
10 MPa (gauge), and more preferably 10 kPa (gauge) to 1 MPa (gauge).
If the pressure is smaller than 1 kPa (gauge), almost no target alkenyl
compounds can be obtained by the reaction. If it is larger than 30 MPa
(gauge), on the other hand, side-reaction products may be produced. The
required pressure can be realized by the vapor pressure of the raw
material compounds, for example, by heating alkylbenzene above its boiling
point or by feeding 1,3-butadiene to the reaction system in a quantity
greater than the quantity required for the reaction. Alternatively,
feeding an inert gas can provide a desired pressure.
The molar ratio of alkylbenzene and 1,3-butadiene used in the reaction
using the above-described catalyst and under the above-described pressure
is suitably selected from the normal range; e.g., the approximate ratio of
alkylbenzene:1,3-butadiene may be 1:0.001 to 1:0.5, preferably 1:0.01 to
1:0.4, and more preferably 1:0.05 to 1:0.3. The amount of alkylbenzene
used as the solvent for the above-described dispersion treatment of
metallic sodium and the specific catalyst component is accounted for this
ratio of alkylbenzene and 1,3-butadiene.
It is desirable that the reaction of alkylbenzene and 1,3-butadiene in the
process of the present invention be carried out substantially in the
absence of water and oxygen. Water may convert metallic sodium into sodium
hydroxide, resulting in decrease in its catalytic activity, and oxygen may
deactivate the catalyst.
Therefore, the raw materials to be charged to the reaction system, i.e.
alkylbenzene and 1,3-butadiene, are desirably those dehydrated.
Further, in order to avoid the presence of substantial amount of oxygen and
water in the open spaces of the reaction system, it is desirable to fill
the open spaces with dry inert gas, such as dry nitrogen or dry argon, or
with the vapor of alkylbenzene or the like, when the reaction is carried
out under pressurized reaction conditions above the boiling point of the
alkylbenzene.
The reaction temperature in the process of the present invention is
preferably about 50.degree. C. to 200.degree. C. If the temperature is
lower than 50.degree. C., by-products may be produced or it takes a longer
period of time for the reaction. If it is higher than 200.degree. C.,
production of the other by-products may increase. The reaction temperature
from 80.degree. C. to 180.degree. C. is preferred.
The reaction time in the range of 0.05 to 10 hours is preferably
applicable. The reaction time is dependent on the amount of the catalyst
(g-catalyst), the composition of the catalyst (g-metallic sodium,
g-specific catalyst component), the reaction temperature (.degree.C.), the
molar ratio of alkylbenzene and 1,3-butadiene
(mol-alkylbenzene/mol-1,3-butadiene), the method of reaction (e.g. the
batch reaction, the continuous reaction, etc. which will be hereinafter
described), and the like. An appropriate reaction time is determined
taking the purity of the target compounds, the manner in which the
catalyst is used (e.g. adoption of catalyst recycle), and the like into
consideration.
Generally, the reaction time is longer as the values for these factors
decrease. The preferable reaction time is 0.1 to 8 hours, and particularly
0.3 to 5 hours.
Any reaction methods may be employed for the reaction in the process of the
present invention. Such reaction methods include batch reaction in which
the raw materials (alkylbenzene and 1,3-butadiene) and the catalyst,
comprising metallic sodium or the combination of metallic sodium and the
specific catalyst component, are charged altogether and reacted;
semi-batch reaction in which alkylbenzene and the catalyst is first
charged to the reactor and 1,3-butadiene is added as the reaction
proceeds; continuous reaction in which alkylbenzene, 1,3-butadiene, and
the catalyst are continuously charged to the reactor; and the
reaction-distillation method in which alkylbenzene and 1,3-butadiene are
introduced to the upper and lower parts, respectively, of a reactor column
filled with the catalyst, and the target reaction products flow down to
the bottom (illustrated hereinafter in more detail in reference to FIG.
1). Any suitable combinations of these methods can be also employed. Among
these, the semi-batch reaction, the continuous reaction, or the
reaction-distillation method are preferred, in order to suppress
production of by-products such as 1,3-butadiene polymers or two or more
mols of 1,3-butadiene addition compounds to alkylbenzene.
In the case of the continuous reaction, either of the following two methods
can be employed due to the use of the solid catalyst. One is the method of
feeding alkylbenzene continuously to the fixed catalyst bed, while
introducing 1,3-butadiene to the alkylbenzene. The other method is
effecting reaction while dispersing the catalyst with stirring in the
reaction system consisting of alkylbenzene and 1,3-butadiene.
Any types of reactors, such as tubular-type, column-type, and vessel-type
reactors, may be used for the continuous reaction.
One of the preferred manners of carrying out the continuous reaction is the
crossing-flow type reaction method in which a plural number of reaction
zones are provided and 1,3-butadiene is quantitatively fed to each
reaction zone.
There are no specific limitations as to the reaction procedure inasmuch as
alkylbenzene and 1,3-butadiene are sufficiently mixed and caused to come
into contact with the catalyst, provided that in the case where
1,3-butadiene is introduced to the reaction system in which the catalyst
is present, it is desirable to introduce alkylbenzene and 1,3-butadiene as
a mixture, for example, as a liquid mixture consisting of liquid
alkylbenzene and liquid 1,3-butadiene or as a vapor-liquid mixture
consisting of gaseous 1,3-butadiene and liquid alkylbenzene. This is to
prevent the inlet port from being choked up by rubber-like or resinous
substance which are considered to be polymers of 1,3-butadiene. An
alternative method of avoiding the choke-up is supplying 1,3-butadiene
directly to the space where the reaction is taking place so as to ensure
absorption and reaction of the 1,3-butadiene on the surface of reactants
in which the catalyst is present.
Further, it is possible to introduce 1,3-butadiene by injection carried on
a carrier gas. Injection can also provide the effect of agitation. An
inert gas from which oxygen and water have been removed, such as nitrogen
or argon, is preferably used here.
This reaction is preferably carried out under agitation. Introduction of
gaseous 1,3-butadiene may provide the effect of agitation. The degree of
agitation should be sufficient for homogeneously dispersing the catalyst
throughout the reactor and for homogeneously mixing the raw materials and
the products.
When the reaction is carried out in a liquid phase dispersion reaction
system, the used catalyst may be separated by a known method, such as
centrifugal precipitation, gravity precipitation, solid phase separation
from a liquid-solid mixture at a low temperature (e.g. filtration,
centrifuge), or the like.
The catalyst recovered can be recycled for reuse. Because the metallic
sodium catalyst is converted into sodium hydroxide and loses the catalytic
activity, fresh metallic sodium corresponding to the lost quantity is
added to the catalyst before recycling for reuse.
In the case of the catalyst comprising metallic sodium and the specific
catalyst component, the layer of the specific catalyst component is
covered by the deactivated sodium hydroxide. Such a catalyst is oxidized
and calcined to burn the organic substances attached thereto and to
convert sodium hydroxide into sodium carbonate, following which the
catalyst is regenerated for reuse by the addition of metallic sodium.
In the reaction-distillation method, the reaction time may be longer than
the above-described reaction time, because it is difficult that two or
more mols of 1,3-butadiene adduct to alkylbenzene, which is one type of
the by-products, is produced by the reaction-distillation method. The
reaction time in the reaction-distillation method can be determined
chiefly from the feed rate of 1,3-butadiene and the catalyst fill length
of the column.
The reaction-distillation method is now illustrated in detail referring to
FIG. 1.
In FIG. 1, the catalyst is filled in the part 11 of the distillation column
10. The raw material alkylbenzene is supplied via line 1. This fresh
alkylbenzene is combined with the unreacted alkylbenzene, which flows out
from line 4 at the top of the column as effluent, is condensed in
condenser 13, and sent via line 5 to vapor-liquid separator 14, where it
is separated from unreacted 1,3-butadiene, which is drawn out from line 6.
The alkylbenzene is then fed to column 10 from the top.
On the other hand, 1,3-butadiene is charged via line 2 to the lowest part
of catalyst-fill section 11 of column 10 in gaseous or liquid state and
caused to come into contact with alkylbenzene while it moves up to the top
of the column, thereby producing an alkenyl compound.
Because the alkenyl compound produced has a boiling point higher than both
alkylbenzene and 1,3-butadiene, it is liquid at temperatures at which
alkylbenzene is present as both the vapor and the liquid. Thus, almost all
alkenyl compound flows down to the bottom of the column.
This bottom product is drawn out from line 8 and sent to reboiler 12, where
it is heated above the temperature at which the alkylbenzene is completely
vaporized, but lower than the temperature at which all of the target
alkenyl aromatic compound is vaporized, and sent back to
reaction-distillation column 10 via line 9. The other portion of the
column bottom product is cooled in cooler 15 and collected as the alkenyl
compound product via line 3.
The pressure in the above reaction system is controlled in the range
specified in the present invention, i.e. between 1 kPa (gauge) and 30 MPa
(gauge), by the pressure-holding valve 16 which is provided in line 6.
Because the product from this reaction system once separated has no chance
of coming into contact with 1,3-butadiene as in the case of the batch
reaction system, the fluid collected via line 3 consists only of alkenyl
aromatic compound which does not substantially contain unreacted
alkylbenzene or by-produced di- or more substituents.
According to the process of the present invention, 5-phenylpentene is
synthesized from toluene; 5-(o-tolyl)-pentene from o-xylene;
5-(p-tolyl)pentene from p-xylene; 5-(m-tolyl)pentene from m-xylene; and
5-(phenyl)hexene from ethylbenzene.
Japanese Patent Application No. 190080/1994 filed on Jul. 20, 1994 and No.
336045/1994 filed on Dec. 22, 1994 are herein incorporated as references.
Other features of the invention will become apparent in the course of the
following description of the exemplary embodiments which are given for
illustration of the invention and are not intended to be limiting thereof.
EXAMPLES
Example 1
0.45 part by weight of metallic sodium and 200 parts by weight of o-xylene
were charged to a 500 ml pressure autoclave equipped with a stirrer having
half-moon-shaped blades. After stirring at 500 rpm at 140.degree. C. for
one hour, the temperature was raised to 150.degree. C. and argon gas was
introduced to bring the pressure to 100 kPa (gauge). 1,3-butadiene was
then introduced at a flow rate of 27.0 ml/min for 3 hours.
The reaction mixture was cooled to 100.degree. C. immediately after the
reaction to separate the metallic sodium from the reaction solution. After
washing with distilled water until the mixture is neutralized, the excess
amount of o-xylene was evaporated, and the residue was distilled under
reduced pressure to obtain 5-(o-tolyl)-pentene. The yield and purity of
the 5-(o-tolyl)pentene was measured. The results are shown in Table 1.
Examples 2-15, Comparative Examples 1-2
5-(o-tolyl)pentene was prepared in the same manner as in Example 1,
provided that the composition of the catalyst, reaction pressure and
temperature listed in Table 1 were employed, and further that the stirring
was carried out at rotation of 1200 rpm for Comparative Examples 1-2.
The yield and purity of the 5-(o-tolyl)pentene were measured. The results
are shown in Table 1.
TABLE 1
__________________________________________________________________________
Reaction Reaction
Reaction
Catalyst
Product
pressure temperature
time Metallic
Yield
Purity
kPa (gauge) (.degree.C.)
(hour)
Na (wt %)*
(%)
(%)
__________________________________________________________________________
Example
1 100 150 3 0.23 85 99
2 100 150 1.5 0.23 91 99
3 100 150 6 0.23 78 99
4 100 150 14 0.23 65 98
5 100 140 3 0.23 85 99
6 200 140 3 0.23 85 99
7 200 140 3 0.10 85 99
8 200 140 3 0.08 84 99
9 200 160 3 0.23 84 98
10 400 120 3 0.20 86 99
11 1000 120 3 0.20 82 98
12 20000 105 3 0.10 63 96
13 10 140 3 0.23 57 98
14 100 140 3 2.00 85 99
15 100 150 3 0.005
78 98
Comparative
Example
1 0 140 3 0.23 0 --
2 0 145 3 0.23 0 --
__________________________________________________________________________
*Na wt % is based for the amount of alkylbenzene.
It is clear from Table 1 that the target 5-(o-tolyl)pentene can be prepared
at a high yield by the process of the present invention. Examples 16-25,
Comparative Examples 3-4
5-(p-tolyl)pentene was prepared in the same manner as in Example 1, except
that p-xylene was used instead of o-xylene and the catalysts with the
composition shown in Table 2 were used.
The yield and purity of the 5-(p-tolyl)pentene were measured. The results
are shown in Table 2.
TABLE 2
__________________________________________________________________________
Reaction Reaction
Reaction
Catalyst
Product
pressure temperature
time Metallic
Yield
Purity
kPa (gauge) (.degree.C.)
(hour)
Na (wt %)*
(%)
(%)
__________________________________________________________________________
Example
16 100 150 3 0.23 86 99
17 100 150 1.5 0.23 92 99
18 100 150 7 0.23 75 98
19 200 140 3 0.20 85 99
20 100 150 3 0.10 85 99
21 100 120 3 0.23 83 98
22 10 150 3 0.20 49 99
23 100 140 3 0.005
80 98
24 20000 105 3 0.10 57 98
25 100 150 3 2.00 85 99
Comparative
Example
3 0 140 3 0.23 0 --
4 0 145 3 0.23 0 --
__________________________________________________________________________
*Na wt % is based for the amount of alkylbenzene.
It is clear from Table 2 that the target 5-(p-tolyl)pentene can be prepared
at a high yield by the process of the present invention.
Examples 26-27
5-(m-tolyl)pentene or 5-(phenyl)hexane was prepared in the same manner as
in Example 1, except that m-xylene (Example 26) or ethylbenzene (Example
27) was used instead of o-xylene.
The yield and purity of the 5-(m-tolyl)pentene or 5-(phenyl)hexane were
measured. The results are shown in Table 3.
TABLE 3
______________________________________
Product
Raw material
Yield (%)
Purity (%)
______________________________________
Example 26 m-Xylene 83 98
Example 26 Ethylbenzene 85 99
______________________________________
Example 28
0.45 part by weight of metallic sodium, 15.0 parts by weight of potassium
carbonate, and 200 parts by weight of o-xylene were charged to a 500 ml
pressure autoclave equipped with a stirrer having half-moon-shaped blades.
After stirring at 500 rpm at 140.degree. C. for one hour, the temperature
was raised to 150.degree. C. and argon gas was introduced to bring the
pressure to 100 kPa (gauge). 1,3-butadiene was then introduced at a flow
rate of 27.0 ml/min for 3 hours.
The reaction mixture was cooled to 100.degree. C. immediately after the
reaction to separate the catalyst from the reaction solution. After
washing with distilled water until the mixture was neutralized, the excess
amount of o-xylene was evaporated, and the residue was distilled under
reduced pressure to obtain 5-(o-tolyl)-pentene. The yield and purity of
the 5-(o-tolyl)pentene was measured. The results are shown in Table 4.
Examples 29-32, Comparative Example 5
5-(o-tolyl)pentene was prepared in the same manner as in Example 28,
provided that the composition of the catalyst, reaction pressure and
temperature listed in Table 4 were employed, and further that the stirring
was carried out at a rotation of 1200 rpm for Comparative Example 5.
The yield and purity of the 5-(o-tolyl)pentene were measured. The results
are shown in Table 4.
TABLE 4
__________________________________________________________________________
Reaction Reaction
Catalyst* Product
pressure temp.
Metallic
Specific Yield
Purity
kPa (gauge) (.degree.C.)
sodium
cat. component
(%) (%)
__________________________________________________________________________
Example
28 100 150 0.23
(K.sub.2 CO.sub.3)
72.0
99
7.5
29 40 140 0.23
(K.sub.2 CO.sub.3)
49.0
99
7.5
30 100 150 0.23
(K.sub.2 CO.sub.3)
(Rb.sub.2 CO.sub.3)
69.0
98
2.5 5.0
31 50 145 0.23
(K.sub.2 CO.sub.3)
(KOH)
70.0
99
5.0 2.5
32 1000 140 0.23
(K.sub.2 CO.sub.3)
78.0
97
7.5
Comparative
Example
5 0 145 0.23
(K.sub.2 CO.sub.3)
2.0
--
7.5 or less
__________________________________________________________________________
*The amounts indicates wt % for the amount of alkylbenzene.
It is clear from Table 4 that the target 5-(p-tolyl)pentene can be prepared
at a high yield by the process of the present invention.
Examples 33-35, Comparative Example 6
5-(p-tolyl)pentene was prepared in the same manner as in Example 28, except
that p-xylene was used instead of o-xylene and the catalysts with the
composition shown in Table 5 were used.
The yield and purity of the 5-(p-tolyl)pentene were measured. The results
are shown in Table 5.
TABLE 5
__________________________________________________________________________
Reaction Reaction
Catalyst* Product
pressure temp.
Metallic
Specific Yield
Purity
kPa (gauge) (.degree.C.)
sodium
cat. component
(%) (%)
__________________________________________________________________________
Example
33 150 150 0.23
(K.sub.2 CO.sub.3)
71.5
99
7.5
34 100 150 0.23
(K.sub.2 CO.sub.3)
(KOH)
69.5
98
5.0 2.5
35 50 145 0.23
(K.sub.2 CO.sub.3)
70.0
99
7.5
Comparative
Example
6 0 145 0.23
(K.sub.2 CO.sub.3)
2.0
--
7.5 or less
__________________________________________________________________________
*The amount indicates wt % for the amount of alkylbenzene.
It is clear from Table 5 that the target 5-(p-tolyl)pentene can be prepared
at a high yield by the process of the present invention.
Example 36
(1) Preparation of a dispersion solution of metallic sodium
2 parts by weight of metallic sodium was charged to 100 parts of by weight
of o-xylene, of which the water content was reduced to below 0.1 ppm with
zeolite in advance. The metallic sodium was finely pulverized by a
mechanical stirrer at 120.degree. C. under high purity nitrogen
atmosphere.
(2) Preparation of a potassium-type Y-zeolite carrier
A commercially available proton-type Y-zeolite was suspended in water. An
aqueous solution of potassium hydroxide (1N) was added dropwise to the
suspension to make the pH 12, following which the suspension was filtered
and sufficiently washed, thus obtaining a potassium-type Y-zeolite.
Dry boehmite alumina in an amount of 20 parts by weight, as aluminum oxide,
was added to 80 parts by weight of the potassium-type Y-zeolite which was
dried at 130.degree. C. The mixture was thoroughly blended, deflocculated
with the addition of 1N aqueous solution of nitric acid, and neutralized
with ammonia water. The clay-like material thus obtained was molded into
rings. The molded products were dried at 130.degree. C. and calcined at
550.degree. C. to obtain rings with an outer size of 3 mm.phi..times.3 mm.
(3) Preparation of a metallic sodium-potassium type Y-zeolite carrier
composite
10 parts by weight of the sodium-potassium type Y-zeolite carrier prepared
in (2) above, was added to 100 parts by weight of o-xylene with a water
content of below 0.1 ppm. To the mixture was added 100 parts by weight of
the dispersion of metallic sodium prepared in (1) above, and the resulting
mixture was stirred at a high speed with a mechanical stirrer, followed by
evaporation of o-xylene.
(4) Synthesis of 5-(o-tolyl)pentene
The metallic sodium-potassium type Y-zeolite carrier composite prepared in
(3) was transferred to a packing column (30 mm.phi..times.500 mm) of a
distillation device equipped with this column and a 1000 ml three-necked
flask, to fill out the upper 60% area of the column (an amount as
catalyst: 200 ml). A coil filler (Helipack, trademark, manufactured by
Nitto Han-noki Co.) was filled in the remaining part of the column.
300 ml of o-xylene with a water content of below 0.1 ppm was charged to the
three-necked flask and heated to the boiling point, thereby evaporating
o-xylene vapor up to the column top. The pressure was raised to 50 kPa
(gauge) and the system was stabilized, while refluxing the whole amount.
Then, 1,3-butadiene was supplied from one of the ports of the three-necked
flask at a rate of 10 ml/min.
After reacting for 3 hours in this manner, o-xylene was evaporated under
reduced pressure to obtain 5-(o-tolyl)pentene. The yield and purity of
5-(o-tolyl)pentene were analyzed. The results shown in Table 6.
Example 37
The same experiment as in Example 36 was carried out, except that in the
preparation of the sodium-potassium type Y-zeolite carrier prepared in
Example 36 (2) a potassium carbonate powder was used instead of the
potassium-type Y-zeolite and aluminum hydroxide gel was used instead of
the dry boehmite alumina. The results are shown in Table 6.
Examples 38-39
The same experiment as in Example 36 was carried out, except that m-xylene
(Example 38) or p-xylene (Example 39) was used instead of o-xylene.
The results are shown in Table 6.
TABLE 6
______________________________________
Product
Raw material
Yield (%)
Purity (%)
______________________________________
Example 36 o-Xylene 75.0 98
Example 37 o-Xylene 73.5 98
Example 38 m-Xylene 72.5 98
Example 39 p-Xylene 69.0 98
______________________________________
Example 40
The same apparatus as used in Example 36(4) was used, except for using a
300 ml flask in the bottom. 50 ml of 5-(o-tolyl)pentene, prepared in
advance, was charged and heated to the boiling point to vaporize
5-(o-tolyl)pentene up to the top of the column and to reflux the whole
amount.
Then, o-xylene was fed from the bottom of the distillation column at a flow
rate of 100 ml (liquid)/hour, while heating the flask to 150.degree. C. (a
temperature above the boiling point of o-xylene) so as to prevent the
o-xylene from coming down to the flask. The pressure was raised to 50 kPa
(gauge). After the system was stabilized, 1,3-butadiene was fed from one
of the ports of the three-necked flask at a rate of 600 ml (gas )/hour.
Feeding the raw materials was terminated after a two hour reaction. Then,
after evaporating o-xylene in the distillation column, the flask was
cooled and its content was weighed, to find that the weight of the product
was 58.5 g (60 ml). The purity of the 5-(o-tolyl)pentene was 99%.
Based on the results, the amount of 5-(o-tolyl)pentene produced (excluding
the initially charged 5-(o-tolyl)pentene) in the reaction for two hours
was found to be 8.5 g, confirming that almost 100% of the 1,3-butadiene
charged was converted into the target product.
The process of the present invention exhibits the following effects.
(1) It is possible to manufacture alkenyl compounds very efficiently at a
greatly increased yield.
(2) It is possible to carry out a highly active and selective alkenylation
reaction at a low cost by employing a specified reaction pressure and
using the catalyst which is easy to handle.
(3) The production of unwanted side reaction products which are difficult
to separate from the target compound can be suppressed. Thus, a high
purity target product can be obtained at a high yield.
(4) The catalyst components used are inexpensive, safe, free from any
danger, and readily separable from the reaction mixture. There are no need
for the use of components such as metallic sodium-potassium alloy which is
expensive, has a risk of being ignited, and is difficult to separate from
the reaction mixture.
Obviously, numerous modifications and variations of the present invention
are possible in light of the above teachings. It is therefore to be
understood that within the scope of the appended claims, the invention may
be practiced otherwise than as specifically described herein.
Top